Regulatory Affairs Specialist

AbbVie

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profile Job Location:

Montevideo - Uruguay

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Mission 

The mission of the Oncology and Specialty Regulatory Affairs Specialist is to be responsible for the regulatory activities related to oncology and specialty products in Paraguay and Uruguay aligned to business needs to assure compliance with local regulations and with AbbVie policies. The Co-technical director is AbbVies representative before the regulatory authorities in Uruguay as well as the link with the representative in Paraguay.

Main responsibilities

1. Regulatory Affairs activities

Devise regulatory strategies aligned within the Brand Team for successfully registering oncology and

specialty products in Uruguay and Paraguay.

Be AbbVies representative before the MSP (local HA) as Co-Technical Director. The technical director and

his deputy are legally liable in solidarity with the company using her or his signature to back up not only

the filings but also the importation and exportation of products and the release of such products to the

internal market.

Execution and follow up of activities related to products life cycle (renewals variations withdrawals

launches etc.).

Lead the interaction with distributor in Paraguay (RA personnel) to assure successful and on time

registrations and business continuity training the regulatory affairs personnel of the distributor and

preparing the regulatory documents for submission.

Management of artworks related activities.

Management of regulatory audits (preparation execution resolution).

Work with area teams in special projects representing Uruguay and Paraguay.

2. Business Support

Participate in Brand Teams as an active member proposing and giving regulatory insights and providing

regulatory intelligence

3. Regulatory Intelligence

Keep the affiliate and region informed of new regulations with impact on the business


Qualifications :

 

Bachelors as a Pharmacist or correlated areas

Minimum 5 years experience in Regulatory Affairs

Knowledge of applicable regulations both for Uruguay and Paraguay

Negotiation skills

English: working level as minimum

Trained in applicable local and international policies and procedures

Team management skills

Good communications skills


Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No


Employment Type :

Full-time

Mission The mission of the Oncology and Specialty Regulatory Affairs Specialist is to be responsible for the regulatory activities related to oncology and specialty products in Paraguay and Uruguay aligned to business needs to assure compliance with local regulations and with AbbVie policies. The Co...
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About Company

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AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

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